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2020 Bio/Pharma Virtual Congress
*** Live: Wednesday, November 11, 2020 | 8:30 AM EDT – 4:00 PM EDT *** 2020 Bio/Pharma Virtual Congress: Join Pharmaceutical Technology® and BioPharm International® for this online event that will explore the latest developments in formulation, manufacturing, and innovative drug dosage forms, as well as detailed discussions about crucial topics impacting the industry. ***On demand available after final airing until 11/11/2021
Advancing the CMC Development of Oncology Medicines
November 2nd 2020***Live: Tuesday, November 17, 2020 at 11am EDT| 8am PDT| 4pm GMT| 5pm CET***Oncology drugs dominate today’s industry pipeline, increasing the pressure on pharmaceutical scientists to get medications to patients as quickly as possible. But does the focus on speed mean sacrifices are made elsewhere in the development plan? Drug developers need to be mindful of the development challenges that come with oncology drug products in order to accelerate to proof-of-concept and onwards towards a successful commercial launch. *** On demand available after final airing until Nov. 17, 2021.***
Manufacturing Technology: Capabilities for Changing Environments
October 29th 2020***Live: Monday, November 16, 2020 at 1pm EST| 12pm CST| 10am PST*** Register for “Manufacturing Technology: Capabilities for Changing Environments.” Learn how pharmaceutical companies have adjusted in response to the COVID-19 pandemic and continued to grow their business. Join us to explore new technology tools that bridge manufacturing and quality while providing data driven insights for better business decisions. *** On demand available after final airing until Nov. 16, 2021.***
Advancing the Pharmaceutical Development of Orphan Drugs for Rare Diseases
October 28th 2020***Live: Wednesday, October 28, 2020 at 11am EDT| 8am PDT| 3pm GMT| 4pm CET*** With over 300 million people worldwide living with one or more identified rare diseases, the development of new treatments to address these unmet clinical needs is an area of significant focus in the pharmaceutical industry. But does the focus on speed mean sacrifices have to be made elsewhere in the development plan for orphan drugs? ***On demand available after final airing until Oct. 28, 2021***
Easy Coloring for Liquid- and Solid-Dosage Drug Forms
October 27th 2020***Live: Tuesday, November 24, 2020 at 9am EST| 2pm GMT| 3pm CET*** Coloring as an aesthetic value for a product is becoming more important for pharmaceutical and nutritional products and helps differentiate between various grades of active ingredients. This webcast introduces the world of easy coloring, answers questions about pigments, pigment blends, and how to color solid- or liquid-dosage forms in an efficient way. Register for this webcast to learn how ready-to-use coloring systems can simplify production process.*** On demand available after final airing until Nov. 24, 2021.***
Formulation Strategies for Early-Phase Clinical Studies
October 27th 2020***Live: November 12, 2020, 11am EST| 8am PST| 4pm GMT| 5pm CET***Formulation strategies for orally administered small molecules can vary widely for early-phase clinical studies and are not always optimal. Sponsors have a wide range of formulation options as they develop program strategies. This webinar will discuss formulation strategies and the advantages that may depend upon drug properties, dosing requirements, and corporate business strategy.*** On demand available after final airing until Nov. 12, 2021.***
Particles, Powders and Pills – Optimized Raman across the Formulation Spectrum
October 22nd 2020***Live:Friday, November 13, 2020 at 11am EST| 8am PST| 4pm GMT| 5pm CET *** From contaminants in injectables to the fate of APIs in nasal sprays, Raman reveals the identity and distribution of materials in complex formulations. In this webinar we describe the best approaches to characterizing common pharmaceutical samples; from morphologically targeted analysis of filtered particles to full three-dimensional chemical imaging of whole tablets.*** On demand available after final airing until Nov. 13, 2021.***
Applying Visual Techniques to the Product Design of Lipid Multiparticulates
October 20th 2020***Live: Friday, November 20, 2020 at 11am EST| 8am PST| 4pm GMT| 5pm CET*** Lipid multiarticulate (LMPs) are versatile drug delivery systems which offer flexibility in both drug release and final dosage form. This webinar discusses the process for formulation selection and LMP manufacturing through the lens of visual techniques.*** On demand available after final airing until Nov. 20, 2021.***
Using Quality Principles to Analyze and Quantify Particulate Matter in Parenteral Packaging
October 20th 2020Do you have concerns about particulate matter entering your parenteral drug product? Register for the Oct. 20 webcast, “Using Quality Principles to Analyze and Quantify Particulate Matter in Parenteral Packaging”. This webcast is part of a series focusing on The Path to Patient Safety: Addressing Industry Concerns and Solutions for Primary Packaging Component Selection. Live: Part III: Tuesday, Oct. 20, 2020 at 10am EDT | 9am CDT | 3pm BST | 4pm CEST On demand available after airing until Oct. 20, 2021 Register free
Overcome N-Nitrosamine Analysis Challenges with Chromatographic and Mass Spectrometry Techniques
October 15th 2020***Live: Monday, Oct. 19, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST*** Learn about the challenges of N-nitrosamines analysis and mass spectrometry and complimentary orthogonal mass spectrometry techniques can be used to address these challenges.. *** On demand available after final airing until Oct. 19, 2021.***
Innovative Approaches to CMC Testing Challenges
October 13th 2020***Live: Wednesday, November 18, 2020 at 10am EST | 9am CST | 3pm GMT | 4pm CET *** Scientific leaders from the United States Pharmacopoeia (USP) and Biogen share perspectives on addressing challenges in chemistry, manufacturing, and controls testing, and provide insights and strategies for a successful path from drug development to commercial manufacturing.***On demand available after airing until Nov. 18, 2021
Does Your Clinical Trial Design Satisfy the Needs of Your Patients?
October 8th 2020*** Live: Thursday, November 5, 2020 at 11am EST | 8am PST | 4pm GMT | 5pm CET***At the center of every clinical trial is a patient awaiting treatment. Learn from the experts on how to design a decentralized clinical trial to improve patient recruitment and retention. ***On demand available after final airing until Nov. 5, 2021***
Capable and Compliant XRD in Pharmaceutical Analysis
October 2nd 2020*** Live: Thursday, October 22, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST*** Be sure you’re using the latest XRD sample preparation and measurement strategies while confidently meeting audit trail and compliance requirements. Learn how recent software solutions enable straightforward, compliant pharmaceutical workflows. ***On demand available after final airing until Oct. 22, 2021***
Planning Ahead: Using Phase 2 to Anticipate Phase 3 Clinical Supply Challenges & Solutions
October 1st 2020*** Live: Monday, Oct. 26, 2020, 11am EDT| 8am PDT| 3pm GMT| 4pm CET *** What are typical challenges sponsors encounter during Phase 3 clinical trials? How can advance preparation during Phase 2 help mitigate risks? Learn effective strategies to avoid surprises and problems in late-stage trials from experience clinical trial and supply experts. ***On demand available after final airing until Oct. 26, 2021***
Understanding Polymorphism to De-Risk Drug Development
September 29th 2020*** Live: Thursday, Oct. 15, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST *** Polymorph screening of small-molecule drug candidates enables rational selection of the proper solid form/polymorph for further development. Learn the elements and techniques of polymorph screening is and why performing it thoroughly will help de-risk drug development effort. ***On demand available after final airing until Oct. 15, 2021***
Layer by Layer: The Fundamentals of Multi-Layer Tableting
September 27th 2020***Live: Tuesday, Oct. 27, 2020 *** Multi-layer tableting offers an inexpensive and straightforward solution for a variety of challenging formulations. Learn how multi-layer formulations compare to traditional methods, gain insight to the multi-layer tableting process, and crucial tips to formulating and manufacturing robust multi-layer tablets. ***On demand available after final airing until Oct. 27, 2021***
Solid form screening and its role in drug development
September 10th 2020In this webcast, Michael Grass PhD (Head of Solid Form Services, Global R&D) will present how solid form screening is performed and the importance of this work to drug substance and drug product development. Live: Thursday, Sep. 10, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Sep 10, 2021 Register free
Extractables and Leachables of Biopharmaceutical Container Closure Systems
September 3rd 2020Learn how to navigate the regulatory requirements for extractables and leachables testing for new biologic drug products. Review the essential steps to for study design, extraction, analysis, and reporting of extractables and leachables data in this webcast. Live: Thursday, Sept. 24, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing until Sept. 24, 2021
Improve Pharmaceutical Methods with Automatic Titration
September 1st 2020In this webcast, Brett Lane, Senior Chemist of Lonza’s QC laboratory in Rochester, NY will share his experience modifying titration manual methods to optimize results using autotitration. Live: Wednesday, Sept. 23, 2020 at 1pm EDT | 12pm CDT | 10am PDT On demand available after final airing until Sept. 23, 2021
Active Packaging Reimagined: Novel Technologies to Derisk Drug Product Stability
August 27th 2020Stability and moisture challenges are likely to increase with the development of more potent APIs, larger molecules, and modified-release tablets. Learn about innovative packaging solutions to address the increasing need to protect hydrophilic oral solid doses from moisture and preserve drug stability. Live: Thursday, Sept. 17, 2020 at 11am EDT| 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Sept. 17, 2021
From Candidate to Clinic: Strategies to Accelerate Your Molecule’s Development Path
August 27th 2020Review how data-driven approaches, including physiologically based pharmacokinetic (PBPK) modeling, parallel formulation screening, API sparing techniques, and optimal early dosing strategies can help avoid development pitfalls for small-molecule drug candidates on the path to clinic. Live: Wednesday, Sept. 23, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST On demand available after final airing until Sept. 23, 2021
Building a More Efficient Routine Lab: Approaches to Modernizing HPLC Methods with New Technologies
August 25th 2020Listen and learn as Dr. James Grinias from Rowan University and Dr. Frank Steiner from Thermo Fisher Scientific discuss approaches and considerations to modernizing HPLC methods to increase throughput using superficially porous particles. They also discuss challenges in method transfer and describe new compliant hardware technologies built into the modern HPLC and UHPLC systems. Live: Tuesday, Aug. 25, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing until Aug. 25, 2021
Injectable Implants: Manufacturing Advanced Medicines with Hot-Melt Extrusion
August 24th 2020The promises of the digital lab are enticing but getting there can seem daunting. The good news is that you can start today. It’s simply about implementation, and not waiting for innovation. Live: Tuesday, Sept. 22, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST On demand available after airing until Sept. 22, 2021
